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Response-adapted Total Neoadjuvant Therapy Guided by Induction Chemotherapy in Early- and Intermediate-risk Low Rectal Cancer for Implementation of a Watch-and-wait Strategy

Response-adapted Total Neoadjuvant Therapy Guided by Induction Chemotherapy in Early- and Intermediate-risk Low Rectal Cancer for Implementation of a Watch-and-wait Strategy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07260526
Enrollment
60
Registered
2025-12-03
Start date
2025-10-01
Completion date
2026-10-30
Last updated
2025-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rectal Cancer

Keywords

rectal cancer, total neoadjuvant therapy, watch-and-wait strategy

Brief summary

This study investigates the feasibility of an organ-preserving watch-and-wait strategy in patients with mid-to-low rectal cancer who achieve a good response after total neoadjuvant therapy (TNT). By retrospectively and prospectively analyzing patients who complete TNT following effective induction chemotherapy, the study aims to assess organ preservation rates and evaluate whether non-surgical management can provide comparable oncologic outcomes to radical surgery while improving functional recovery and quality of life.

Detailed description

With the evolution of rectal cancer treatment concepts, achieving optimal oncologic outcomes while preserving organ function and improving patients' quality of life has become a major goal in the management of low rectal cancer. Multiple studies have reported that for patients who achieve a clinical complete response (cCR) after total neoadjuvant therapy (TNT), a watch-and-wait (organ preservation) strategy-with close follow-up and salvage surgery when necessary-yields 5-year disease-free survival (DFS) and overall survival (OS) rates comparable to those of patients who undergo radical surgery and achieve a pathological complete response (pCR). Moreover, compared with total mesorectal excision (TME), patients managed with a watch-and-wait approach demonstrate significantly better physical, cognitive, role, and social-emotional functioning, along with lower incidences of bowel, sexual, and urinary dysfunction. This study aims to retrospectively and prospectively include patients with mid-to-low rectal cancer who respond well to induction chemotherapy and subsequently complete TNT, in order to observe the organ preservation rate after TNT and to preliminarily evaluate the feasibility of this treatment approach within a watch-and-wait strategy.

Interventions

None listed

Sponsors

West China Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age: 18-80 years; no restriction on sex. * Histologically confirmed rectal adenocarcinoma with immunohistochemistry and/or genetic testing showing pMMR/MSS status. * Tumor characteristics assessed by chest-abdominal CT, rectal ultrasound, and MRI meeting all of the following criteria: 1. The lower edge of the tumor is ≤5 cm from the anal verge as measured by digital rectal examination or MRI; 2. Clinical stage cT1-3abN0-1M0 (for cT1N0, patients suitable for endoscopic resection are excluded); 3. MRF (-) (\>1 mm), EMVI (±); 4. Negative lateral lymph nodes and \<7 mm in size; 5. Maximum tumor length ≤5 cm; 6. Tumor circumference involvement ≤2/3. * After receiving at least two cycles of induction chemotherapy with the XELOX regimen, MRI assessment shows treatment response (tumor length reduced by ≥30% compared with baseline). * Completion of total neoadjuvant therapy (TNT), including long-course chemoradiotherapy and consolidation chemotherapy (radiotherapy: 25-28 fractions; chemotherapy: 6-8 cycles). * (For the prospective cohort) Provision of written informed consent for participation in this observational study.

Exclusion criteria

* Patients with a history of, or concurrent, other malignant tumors (except for cured basal cell carcinoma of the skin or carcinoma in situ of the cervix); * Patients with severely incomplete clinical data that preclude effective evaluation; * (For the prospective cohort) Patients who refuse to provide written informed consent.

Design outcomes

Primary

MeasureTime frameDescription
1-year organ preservation rate1 year after completion of neoadjuvant radiotherapydefined as the proportion of the following two groups among the total study population:① Patients evaluated as having a clinical complete response (cCR) or near cCR at 8 weeks after radiotherapy who choose a watch-and-wait strategy and maintain cCR for 1 year; ② Patients evaluated as having a cCR or near cCR at 8 weeks after radiotherapy who ultimately undergo local excision and remain recurrence-free for 1 year without requiring salvage surgery.

Secondary

MeasureTime frameDescription
1-year metastasis-free survival1 year after total neoadjuvant therapytime from the start of neoadjuvant chemotherapy to the occurrence of distant metastasis
1-year overall survival1 year after total neoadjuvant therapytime from the start of neoadjuvant chemotherapy to death from any cause.

Countries

China

Contacts

Primary ContactZiqiang Wang, M.D.
wangziqiang@scu.edu.cn+86 18980602028

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026